• Product name
    Anti-GLE1 antibody
  • Description
    Rabbit polyclonal to GLE1
  • Host species
  • Tested applications
    Suitable for: WB, IHC-P, ICC/IFmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse, Rat, Cow
  • Immunogen

    Recombinant protein fragment corresponding to a region within amino acids 414 and 656 of GLE1.

  • Positive control
    • WB: 293T, A431, HeLa, MOLT4 or Raji cell lysate for WB; ICC/IF: HeLa cells; IHC-P: Cal27 xenograft.



Our Abpromise guarantee covers the use of ab96007 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB 1/500 - 1/3000. Predicted molecular weight: 75 kDa.
IHC-P 1/100 - 1/500.
ICC/IF 1/100 - 1/200.


  • Function
    Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC).
  • Involvement in disease
    Defects in GLE1 are the cause of lethal congenital contracture syndrome type 1 (LCCS1) [MIM:253310]; also known as multiple contracture syndrome type Finnish. LCCS is an autosomal recessive disorder characterized by early fetal hydrops and akinesia, micrognatia, pulmonary hypoplasia, pterygia, multiple joint contractures, specific neuropathology with degeneration of anterior horn neurons and extreme skeletal muscle atrophy. LCCS1 leads to prenatal death.
    Defects in GLE1 are the cause of lethal arthrogryposis with anterior horn cell disease (LAAHD) [MIM:611890]. LAAHD is characterized by fetal akinesia, arthrogryposis and motor neuron loss. LAADH fetus often survive delivery, but die early as a result of respiratory failure. Neuropathological findings resemble those of LCCS1, but are less severe.
  • Sequence similarities
    Belongs to the GLE1 family.
  • Cellular localization
    Nucleus. Cytoplasm. Shuttles between the nucleus and the cytoplasm. Shuttling is essential for its mRNA export function and Cytoplasm. Nucleus > nuclear pore complex. Shuttles between the nucleus and the cytoplasm. In the nucleus, isoform 1 localizes to the nuclear pore complex and nuclear envelope. Shuttling is essential for its mRNA export function.
  • Information by UniProt
  • Database links
  • Alternative names
    • GLE 1 antibody
    • GLE1 antibody
    • GLE1 like protein antibody
    • GLE1 like RNA export mediator antibody
    • GLE1 RNA export mediator homolog antibody
    • GLE1 RNA export mediator like (yeast) antibody
    • GLE1-like protein antibody
    • GLE1_HUMAN antibody
    • GLE1L antibody
    • hGLE1 antibody
    • LCCS 1 antibody
    • LCCS antibody
    • LCCS1 antibody
    • Nucleoporin GLE1 antibody
    see all


  • Anti-GLE1 antibody (ab96007) at 1/1000 dilution + HeLa whole cell lysate at 30 µg

    Predicted band size: 75 kDa

    7.5% SDS PAGE
  • Top panel: immunofluorescence analysis of paraformaldehyde-fixed HeLa cells, using ab96007 at 1/200 dilution.
    Bottom panel: merged with DNA probe.
  • 1/500 ab96007 staining GLE1 in formalin-fixed, paraffin-embedded Cal27 xenograft by immunohistochemistry.


This product has been referenced in:
  • Jao LE  et al. A role for Gle1, a regulator of DEAD-box RNA helicases, at centrosomes and basal bodies. Mol Biol Cell 28:120-127 (2017). Read more (PubMed: 28035044) »
  • Hodroj D  et al. An ATR-dependent function for the Ddx19 RNA helicase in nuclear R-loop metabolism. EMBO J 36:1182-1198 (2017). Read more (PubMed: 28314779) »
See all 3 Publications for this product

Customer reviews and Q&As


I am sorry this product did not perform as stated on the datasheet and for the inconvenience this has caused. As requested, I have issued a free of charge replacement for one vial of ab96007.

To check the status of the order please contact our Customer Service team and reference this number.

Please note that this free of charge replacement vial is also covered by our Abpromise guarantee. Should you still be experiencing difficulties, or if you have any further questions, please do not hesitate to let us know.

I wish you the best of luck with your research.

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